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gavmur [86]
3 years ago
15

What is the main difference between a taproot and a fibrous root?

Biology
1 answer:
anastassius [24]3 years ago
5 0
Fibrous roots grow from the main stem of the plant and does not have a primary root like the taproot. They grow downward and outward, with repeating branches to form a mass of small roots.Dicots and monocots are the two classes of flowering plants. The majority of taproot systems are composed of dicots and conifers.
You might be interested in
If the marginal propensity to save is 0.25, a $15 billion increase in government spending will lead to an increase in national i
Greeley [361]

Based on the marginal propensity to save, MPS , the national income will increase by a maximum of $20 billion.

<h3>What is marginal propensity to save?</h3>

Marginal propensity to save (MPS) is a measure of how savings will change, given a change in income.

Marginal propensity to save is related to marginal propensity to consume, MPC by the formula:

  • MPS + MPC = 1

Grom the given value of MPS,

MPC = 1 - 0.25

Therefore, MPC = 0.75

Also, the formula for calculating marginal propensity to consume is given as:

  • Marginal propensity, MPC = ΔC/ΔY

Where:

  • ΔC is a change in consumption
  • ΔY is a change in income

ΔY = ΔC/MPC

ΔY = $15 billion/0.75

ΔY = $20 billion

Therefore, the national income will increase by a maximum of $20 billion.

Learn more about marginal propensity to save at: brainly.com/question/18521055

4 0
2 years ago
A man with the autosomal recessive disorder phenylketonuria (PKU) and a woman without PKu heve a son named Peter, who does not h
Anton [14]

Answer:

<h2>2. Peter's maternal grandfather has PKU.</h2>

Explanation:

  • Such type of the genetic disorder in which two copies of a gene must be mutated at a time is called autosomal recessive disorder such as sickle cell anemia, phenylketonuria, and some other diseases.
  • When a sing copy of a gene is mutated in a person then this disorder is not appeared and the person is called a carrier.
  •  So when a child is born by two carrier parents then there is a chance that a child will be affected if both the parents donate mutated genes.
  • In the case of Peter, since peter does not show this defect this means his maternal grandfather was affected by this disorder.

5 0
3 years ago
What are the nonliving components of the environment that shape an ecosystem?
katrin [286]
The best answer to the question 'What are the nonliving components of the environment that shape an ecosystem?' would be letter d. Abiotic factors are those components of the environment that are non-living or does not have life. All the other choices have life.
4 0
3 years ago
Lesch-Nyhan syndrome is an X-linked, recessive condition caused by mutation of the HPRT1 gene responsible for purine metabolism.
Elanso [62]

Answer:

B. The father did not contribute a sex chromosome to his daughter due to nondisjunction of the sex chromosomes. The daughter is XO and her only X chromosome came from her mother, who was a carrier.

A.The mother's X chromosomes failed to separate during meiosis, and the daughter inherited two X chromosomes with the Lesch-Nyhan mutation. The father contributed no sex chromosomes.

Explanation:

As seen in the question above, a little girl was diagnosed with Lesch-Nyhan syndrome, which is an X-linked recessive condition caused by a mutation in the HPRT1 gene responsible for purine metabolism.

The little girl's parents do not have the syndrome, and no one in the little girl's paternal family presented this syndrome, however, we know that the maternal grandfather of the little girl's mother had the syndrome, which means that it was the mother's genetic material that contributed to the development of the syndrome in the little girl. This was because the little girl did not receive any X chromosomes from her father, but she inherited the two X chromosomes from her mother that coded for the Lesch-Nyhan mutation. This happened because the mother's X chromosome disjuction did not occur during meiosis I.

As shown above, the father did not contribute any sex chromosomes to his daughter, which means that the daughter is XO and her only X chromosome came from her mother, who was a carrier.

3 0
2 years ago
Identify the evolutionary forces that can cause allele frequencies to change from one generation to the next.
Irina-Kira [14]

<u> Allele frequencies to change from one generation to the next.-</u>

<u>B. </u><u>Mutation</u><u>; C. Random genetic drift; D. </u><u>Migration</u><u>; F. Natural selection</u>

  • Selection, mutation, migration, and genetic drift are the mechanisms that effect changes in allele frequencies.
  • When one or more of these forces are acting, the population violates Hardy-Weinberg assumptions, and evolution occurs.

Why do allele frequencies change from one generation to the next?

Random selection: Allele frequencies may fluctuate from one generation to the next when people with particular genotypes outlive those with different genotypes.

No mutation: Allele frequencies may fluctuate from one generation to the next if new alleles are produced via mutation or if alleles mutate at different rates.

What are 5 factors that cause changes in allele frequency?

  • A population, a collection of interacting individuals of a single species, exhibits a change in allele frequency from one generation to the next due to five main processes.
  • These include natural selection, gene flow, genetic drift, and mutation.

Learn more about allele frequency

brainly.com/question/7719918

#SPJ4

<u>The complete question is -</u>

Identify the evolutionary forces that can cause allele frequencies to change from one generation to the next. Check all that apply

A. Inbreeding

B. Mutation,

C. random genetic drift

D. migration

E. extinction

F. natural selection

6 0
1 year ago
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